The evolution of groundwater in the Tyrrell catchment, south-central Murray Basin, Victoria, Australia

The Tyrell catchment lies on the western margin of the Riverine Province in the south-central Murray Basin, one of Australia’s most important groundwater resources. Groundwater from the shallow, unconfined Pliocene Sands aquifer and the underlying Renmark Group aquifer is saline (total dissolved solids up to 150,000 mg/L) and is Na-Cl-Mg type. There is no systematic change in salinity along hydraulic gradients implying that the aquifers are hydraulically connected and mixing during vertical flow is important. Stable isotopes (¹⁸O+²H) and Cl/Br ratios indicate that groundwater is entirely of meteoric origin and salts in this system have largely been derived by evapotranspiration of rainfall with only minor halite dissolution, rock weathering (mainly feldspar dissolution), and ion exchange between Na and Mg on clays. Similarity in chemistry of all groundwater in the catchment implies relative consistency in processes over time, independent of any climatic variation. Groundwater in both the Pliocene Sands and Renmark Group aquifers yield ages of up to 25 ka. The Tyrrell Catchment is arid to semi-arid and has low topography. This has resulted in relatively low recharge rates and hydraulic gradients that have resulted in long groundwater residence times.     

A biogenic-silica δO record of climatic change during the last glacial–interglacial transition in southwestern Alaska

Despite growing evidence for environmental oscillations during the last glacial–interglacial transition from high latitude, terrestrial sites of the North Pacific rim, oxygen-isotopic records of these oscillations remain sparse. The lack of data is due partially to the paucity of lakes that contain carbonate sediment suitable for oxygen-isotopic analysis. We report here the first record of oxygen-isotopic composition in diatom silica (δ¹⁸O_Si) from a lake in that region. δ¹⁸O_Si increases gradually from 19.0 to 23.5‰ between 12,340 and 11,000 ¹⁴C yr B.P., reflecting marked climatic warming at the end of the last glaciation. Around 11,000 ¹⁴C yr B.P., δ¹⁸O_Si decreases by 1.7‰, suggesting a temperature decrease of 3.5–8.9 °C at the onset of the Younger Dryas (YD) in southwestern Alaska. Climatic recovery began ca. 10,740 ¹⁴C yr B.P., as inferred from the increase of δ¹⁸O_Si to a maximum of 23.9‰ near the end of the YD. Our data reveal that a YD climatic reversal in southwestern coastal areas of Alaska occurred, but the YD climate did not return to full-glacial conditions.     

Comparison of source rock geochemistry of selected rocks from the Schei Point group and Ringnes formation, Sverdrup basin, arctic Canada

Organic-rich from the Schei Point group (middle to late Triassic in age) and the Ringnes formation (late Jurassic) from the Sverdrup basin of the Canadian arctic archipelago have been geochemically evaluated for source rock characterization. Most samples from the Schei Point group are organic-rich (> 2% TOC and are considered as immature to mature oil-prone source rocks [kerogen types I, I–II (IIA) and II (IIA)]. These kerogen types contain abundant AOM1, AOM2 and alginite (Tasmanales, Nostocopsis, Leiosphaeridia, acritarch and dinoflagellate) with variable amounts of vitrinite, inertinite and exinite. Samples from the Ringnes formation contain dominant vitrinite and inertinite with partially oxidized AOM2, alginite and exinite forming mostly immature to mature condensate- and gas-prone source rocks [kerogen type II–III (IIB), III and a few II (IIA)]. Schei Point samples contain higher bitumen extract, saturate hydrocarbons and saturate/ aromatic ratio than the Ringnes samples. Triterpane and sterane (dominant C₃₀) distribution patterns and stable carbon isotope of bitumen and kerogen suggest that the analyzed samples from the Schei Point group are at the onset of oil generation and contain a mixture of sapropelic (algal) and minor terrestrial humic organic matter. Sterane carbon number distributions in the Ringnes formation also suggest a mixed algal and terrestrial organic matter type. There are some variations in hopane carbon number distributions, but these are apparently a function of thermal maturity rather than significant genetic differences among samples. Pyrolysis-gas chromatography/mass spectrometry of the two samples with similar maturity shows that the Schei Point sample generates three times more pyrolyzate than the Ringnes sample. Both samples have a dominant aliphatic character, although the Ringnes sample contains phenol and an aromaticity that is higher than that of the Schei Point sample.     

Steady, annual, and monthly recharge implied by deep unconfined aquifer flow

We consider the response of a deep unconfined horizontal aquifer to steady, annual, and monthly recharge. A groundwater divide and a zero head reservoir constrain the aquifer, so that sinusoidal monthly and aperiodic annual recharge fluctuations create transient specific discharge near the reservoir and an unsteady water table elevation inland. One existing and two new long-term data sets from the Plymouth-Carver Aquifer in southeastern Massachusetts calibrate and confirm hydraulic properties in a set of analytical models. [Geohydrology and simulated groundwater flow, 1992] data and a new power law for tritiugenic helium to tritium ratios calibrate the steady recharge that drives the classical parabolic model of steady hydraulics [Applied Hydrogeology, 2001]. Observed water table and gradient fluctuations calibrate the transient recharge models. In the latter regard, monitoring wells within 1 km of Buttermilk Bay exhibit appreciable specific discharge and reduced water table fluctuations. We apply [Trans Am Geophys Union 32(1951)238] periodic model to the monthly hydraulics and a recharge convolution integral [J Hydrol 126(1991)315] to annual flow. An infiltration fraction of 0.79 and a consumptive use coefficient of 1.08×10⁻⁸ m/s °C relate recharge to precipitation and daylight weighted temperature across all three time scales. Errors associated with this recharge relation decrease with increasing time scale.     

中国火山温泉气体地球化学特征及其在火山监测中的应用

中国火山温泉主要分布在吉林长白山、云南腾冲和黑龙江五大连池等火山区。这些火山虽然处于休眠状态,但大面积的温泉分布指示着岩浆房存在的可能性。本文总结了前人研究成果,分析了中国主要火山区温泉气体地球化学特征,并探讨了温泉气体在火山监测中的应用。长白山、腾冲和五大连池火山区温泉气体地球化学性质类似,都以CO₂为主要气体,含量在80%以上,最高可达99%以上,其它气体组分包括CH₄、N₂、O₂、SO₂、H₂S、He和H₂等。长白山火山温泉气体中氦同位素比值（3He/4He）最高,约为4—6R_A,CO₂中碳同位素比值（δ13C）为-7.9‰—-1.3‰,CH₄中碳同位素为-48.0‰—-28.7‰;腾冲火山温泉气体氦同位素比值为3—5.5R_A,CO₂中的碳同位素为-6.49‰—-2.07‰,CH₄中碳同位素为-23.5‰—-9.3‰;五大连池火山温泉气体氦同位素比值约为3R_A,CO₂中的碳同位素比值为-9.6‰—-3.1‰,CH₄中碳同位素为-47.2‰—-44.4‰。3个火山区的温泉气体均显示地幔来源的岩浆气体特征,并在上升运移过程中受地壳或古俯冲物质的影响。     

Carbonatites in a subduction system: The Pleistocene alvikites from Mt. Vulture (southern Italy)

We report here, for the first time, on the new finding of extrusive calciocarbonatite (alvikite) rocks from the Pleistocene Mt. Vulture volcano (southern Italy). These volcanic rocks, which represent an outstanding occurrence in the wider scenario of the Italian potassic magmatism, form lavas, pyroclastic deposits, and feeder dikes exposed on the northern slope of the volcano. The petrography, mineralogy and whole-rock chemistry attest the genuine carbonatitic nature of these rocks, that are characterized by high to very high contents of Sr, Ba, U, LREE, Nb, P, F, Th, high Nb/Ta and LREE/HREE ratios, and low contents of Ti, Zr, K, Rb, Na and Cs. The O–C isotope compositions are close to the “primary igneous carbonatite” field and, thus, are compatible with an ultimate mantle origin for these rocks. The Sr–Nd–Pb–B isotope compositions, measured both in the alvikites and in the silicate volcanic rocks, indicate a close genetic relationship between the alvikites and the associated melilitite/nephelinite rocks. Furthermore, these latter products are geochemically distinct from the main foiditic-phonolitic association of Mt. Vulture. We propose a petrogenetic/geodynamic interpretation which has important implications for understanding the relationships between carbonatites and orogenic activity. In particular, we propose that the studied alvikites are generated through liquid unmixing at crustal levels, starting from nephelinitic or melilititic parent liquids. These latter were produced in a hybrid mantle resulting from the interaction through a vertical slab window, between a metasomatized mantle wedge, moving eastward from the Tyrrhenian/Campanian region, and the local Adriatic mantle. The occurrence of carbonatite rocks at Mt. Vulture, that lies on the leading edge of the Southern Apennines accretionary prism, is taken as an evidence for the carbonatation of the mantle sources of this volcano. We speculate that mantle carbonatation is related to the introduction of sedimentary carbon from the Adriatic lithosphere during Tertiary subduction.     

Enregistrement de la variabilité hydroclimatique au cours des 6500 dernières années sur le littoral de Cabo Frio (Rio de Janeiro,Brésil)

This study concerns a core collected in Brejo do Espinho's lagoon from Cabo Frio littoral (Brazil) submitted to dry influence of local upwelling controlled by north-east trade winds from the South Atlantic and particularly strengthened during El Niño events. Diatoms study supported by sedimentological and isotopic analyses shows dry phases infrequent before 4000 yr, a highly variable climatic phase between 3600 and 2900 yr and from 2400 yr onward a dryness enhancement. To cite this article: B. Laslandes et al., C. R. Geoscience 338 (2006).     

Hydrochemical and isotopic investigation of a sandstone aquifer groundwater in a semi arid region,El Ma El Abiod,Algeria

This work present results of the hydrochemical and isotopic studies on groundwater samples from the study area. Chemical and environmental isotope data are presented and discussed in terms of the origin of dissolved species and of groundwater. All of the investigated groundwater are categorized into two chemical types: low and relatively high mineralized waters type. Interpretation of chemical data, based on both thermodynamic calculations and stability diagrams, suggests that the chemical evolution of groundwater is primarily controlled by water-rock interactions. Interpretation of ¹⁸O and ²H suggests that the recharge of the investigated groundwater may result from differents mechanisms     

碳酸盐沉积物的成岩作用

化学沉淀碳酸盐矿物在沉积后很容易受到各种作用的影响,其中最重要的是其在成岩阶段所经历的成岩作用.碳酸盐沉积物在成岩过程中主要受大气降水、海水和埋藏过程中孔隙流体的控制,经历一系列压实、溶解、矿物的多相转变、重结晶、胶结等成岩作用,逐渐转变为固结的岩石.在成岩过程中,由于孔隙流体与沉积流体之间的异同以及温度的变化,碳酸盐沉积物的原始矿物成分、地球化学特征可能会很好的保存下来,但在许多情况下,也可能会改变,从而使我们无法准确反演碳酸盐沉积物在沉积时水体的特征.因此,我们在应用碳酸盐岩重建相关古环境和古气候变化的时候,必须要通过有效的方法来对碳酸盐岩是否受到成岩作用的影响进行鉴定.     

青藏高原晚始新世干旱化事件：改则盆地康托组碳酸盐岩碳氧同位素的记录

改则盆地位于青藏高原腹地,盆地内沉积物记录了高原古环境变化的重要信息。本文对改则盆地康托组碳酸盐岩碳氧同位素进行研究,结果显示改则盆地中-晚始新世的演化分为两个阶段:1中始新世湿润气候下开放湖盆阶段:虽然碳酸盐岩δ~(18)O值在43层处向正值偏移,但整体~(18)O和~(13)C强烈亏损,并且该时期碳酸盐岩δ~(18)O值和δ~(13)C变化相关系数为R~2=0.082。表明该阶段的研究区虽然经历过短期蒸发作用增强或补给水减少,但整体是气候湿润条件下补给水丰富的开放型湖盆。2晚始新世干旱气候下封闭湖盆阶段:经过中新世晚期(63层)气候和湖泊水文状态的过渡,晚始新世~(18)O和~(13)C同位素富集,δ~(18)O值和δ~(13)C值变化相关系数为R~2=0.7762。表明该阶段气候干旱,蒸发作用强烈,湖盆萎缩成为封闭湖盆。综合前人研究,认为青藏高原腹地及北缘、东北缘在晚始新世存在明显的区域性干旱化事件。对比分析青藏高原隆升、全球气候记录、全球海水Sr和大气CO_2记录,认为青藏高原腹地和北部的干旱化事件主要受青藏高原隆升的影响。